Results 141 to 150 of about 1,434 (204)
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Vitiligo and dysgammaglobulinemia. A case report and family study
Clinical Genetics, 1975This report concerns an 8 year old female with vitiligo and a dysgammaglobulinemia characterized by absent IgA, very low IgG, and normal TgM. The t‐cell immune system was intact but other family members had low levels or absence of IgA. The possible relationship of dysgammaglobulinemia and vitiligo is discussed along with the classification and ...
Warren W. Epinette +3 more
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Dysgammaglobulinemia associated with malabsorption and tetany
The American Journal of Digestive Diseases, 1970 A patient is reported with a malabsorption syndrome associated with nodular lymphoid hyperplasia of the small intestine and dysgammaglobulinemia characterized by virtual absence of IgA and IgM, with a reduced concentration of IgG. Prominent clinical features were severe steatorrhea and tetany.
Fred Anderson +2 more
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Type I dysgammaglobulinemia, systemic lupus erythematosus and lymphoma
The American Journal of Medicine, 1970Abstract There is an increasing body of evidence based upon clinical reports and current concepts of immunopathogenesis that the association among connective tissue disease, immune deficiency and lymphoma is of considerable theoretic as well as practical importance.
C. Kent Smith +2 more
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The immunopathology of spontaneously acquired dysgammaglobulinemia in chickens
Clinical Immunology and Immunopathology, 1980Abstract The acquired immunopathology of lymphoid and parenchymal organs of University of California, Davis (UCD), line 140 White Leghorn chickens, previously demonstrated to have an inherited dysgammaglobulinemia with associated autoimmune phenomena, is described and compared to normal UCD chicken lines 159, 011, and 440.
Kent L. Erickson +6 more
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Gastroenterology, 1986
Primary sclerosing cholangitis is an uncommon disorder of obliterative biliary inflammation that is exceedingly rare in childhood. Presented is a child with hyperimmunoglobulin M immunodeficiency (dysgammaglobulinemia) and primary sclerosing cholangitis.
Jack A. DiPalma +2 more
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Primary sclerosing cholangitis is an uncommon disorder of obliterative biliary inflammation that is exceedingly rare in childhood. Presented is a child with hyperimmunoglobulin M immunodeficiency (dysgammaglobulinemia) and primary sclerosing cholangitis.
Jack A. DiPalma +2 more
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Thymic alymphoplasia, previously reported as dysgammaglobulinemia type I
The Journal of Pediatrics, 1970A child previously reported as having dysgammaglobulinemia type I was also demonstrated to have thymic alymphoplasia. His age and clinical course indicated that his disease was milder than the usual form. This may explain his earlier course, which was somewhat similar to that of Bruton's disease.
Stebbins B. Chandor +2 more
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"Asymptomatic" Type I Dysgammaglobulinemia in Siblings
Annals of Internal Medicine, 1968 Abstract A family with type I dysgammaglobulinemia is presented in which a brother and sister were affected.
John Durant +3 more
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Nodular lymphoid hyperplasia of the small intestine with Burkitt's lymphoma and dysgammaglobulinemia
Gastrointestinal Radiology, 1981 An unusual case of American Burkitt's lymphoma of the jejunum complicating diffuse nodular lymphoid hyperplasia of the small bowel is reported. The radiological and pathological findings are correlated and the pertinent literature is reviewed.
Paul S. Schaefer, Arnold C. Friedman
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Gaucher disease and dysgammaglobulinemia: A report of 61 patients, including 18 with GD type III
Blood Cells, Molecules & Diseases, 2010 Agnieszka Jurecka +4 more
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